Job Summary
IQVIA is in search of a Senior Clinical Research Associate to manage oncology clinical trial sites, focusing on maintaining adherence to protocols and regulatory standards. This position plays a vital role in monitoring sites and ensuring the integrity of Phase 1 cancer studies conducted at various locations.
Responsibilities
- Oversee oncology trial sites to ensure compliance with study protocols.
- Monitor site activities, ensuring adherence to regulatory requirements.
- Support recruitment efforts to enroll participants in clinical trials.
- Provide training and guidance to site staff on study procedures.
- Conduct quality assurance to uphold study integrity throughout the trial process.
Qualifications
- Extensive experience in clinical monitoring, particularly in oncology trials.
- Strong knowledge of clinical research regulations and Good Clinical Practice (GCP).
- Excellent interpersonal and communication skills for effective collaboration with site staff.
- Ability to manage multiple sites and projects in a fast-paced environment.
- Proficiency in problem-solving and decision-making related to trial operations.
IQVIA provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
